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1-(5-(1,2,3,4-tetrahydronaphthalen-6-yl)thiazol-2-yl)-2-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)hydrazine | 1562102-10-6

中文名称
——
中文别名
——
英文名称
1-(5-(1,2,3,4-tetrahydronaphthalen-6-yl)thiazol-2-yl)-2-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)hydrazine
英文别名
——
1-(5-(1,2,3,4-tetrahydronaphthalen-6-yl)thiazol-2-yl)-2-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)hydrazine化学式
CAS
1562102-10-6
化学式
C29H25N5S
mdl
——
分子量
475.617
InChiKey
PESVXOGHRJMABI-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    185-186 °C
  • 沸点:
    700.8±70.0 °C(predicted)
  • 密度:
    1.27±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.99
  • 重原子数:
    35.0
  • 可旋转键数:
    6.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    55.1
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    1-(5-(1,2,3,4-tetrahydronaphthalen-6-yl)thiazol-2-yl)hydrazine1,3-二苯-1H-吡唑-4-甲醛乙醇 为溶剂, 反应 10.0h, 以56%的产率得到1-(5-(1,2,3,4-tetrahydronaphthalen-6-yl)thiazol-2-yl)-2-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)hydrazine
    参考文献:
    名称:
    Synthesis and evaluation of anti-inflammatory and analgesic activity of some substituted thiazolyl and thaizolidinonyl tetrahydronapthalene derivatives
    摘要:
    A new series of 1,2,3,4-tetrahydronaphthalen-6-yl-thiazole and thiazolidinone derivatives were synthesized. Twenty four of the newly synthesized compounds were evaluated for their anti-inflammatory and analgesic activity. The study exhibited that the derivatives 7b and 11c produced equipotent anti-inflammatory activity to that of the reference drug indomethacin with faster onset of action. Meanwhile, the compounds 1b, 1d, 6, 10c, 12c, 12e exhibited interesting dual anti-inflammatory and analgesic activity. The thiazolo-coumarin derivative 6 could be identified as the most biologically active member within this study with a significant dual anti-inflammatory and analgesic activity in comparison with indomethacin. The study of ulcerogenic effects proved that all of the tested compounds revealed super GIT safety profile in the experimental rats.
    DOI:
    10.1007/s00044-014-0926-z
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